Synthetic Access to Secondary Propargylamines via a Copper-Catalyzed Oxidative Deamination/Alkynylation Cascade

A novel and selective cascade reaction of primary amines and alkynes for the synthesis of the corresponding secondary propargylamines is described. This protocol proceeds with a CuBr2/TBHP system through a process of oxidative deamination of primary amines to imine and alkynylation, featuring a wide scope of substrates with good functional-group tolerance and operational simplicity. Additionally, the use of two different primary amines could also work smoothly using this protocol. © 2019 American Chemical Society.

Авторы
Li H.1 , Feng H.1 , Zhang J. 1 , Van Der Eycken E.V. , Huang L.1
Номер выпуска
16
Язык
Английский
Страницы
10501-10508
Статус
Опубликовано
Том
84
Год
2019
Организации
  • 1 College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai, 201620, China
  • 2 Laboratory for Organic and Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, KU Leuven, Celestijnenlaan 200F, Leuven, 3001, Belgium
  • 3 Peoples' Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya Street, Moscow, 117198, Russian Federation
Ключевые слова
Copper; Copper compounds; Alkynylations; Cascade reactions; Copper catalyzed; Oxidative deamination; Primary amines; Propargylamines; Amines; alkyne; amine; copper; functional group; imine; propargylamine; unclassified drug; alkynylation; Article; catalysis; chemical structure; deamination; hydroamination; oxidation; synthesis
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